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All: 61 
OMIM dbSNP: 5 
OMIM UniSTS: 13 
Items 1 - 20 of 61
 
 of 4
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1: #187500 Links
TETRALOGY OF FALLOT
Gene map locus 20p12, 8q23, 5q34
2: 239711 Links
HYPERTELORISM AND TETRALOGY OF FALLOT
3: 187501 Links
TETRALOGY OF FALLOT AND GLAUCOMA
4: 605618 Links
TETRALOGY OF FALLOT SYNDROME, AUTOSOMAL RECESSIVE
5: 601127 Links
FALLOT COMPLEX WITH SEVERE MENTAL AND GROWTH RETARDATION
6: *600584 GeneTests, Links
NK2, DROSOPHILA, HOMOLOG OF, E; NKX2E
Gene map locus 5q34
7: +601920 GeneTests, Links
JAGGED 1; JAG1
DEAFNESS, CONGENITAL HEART DEFECTS, AND POSTERIOR EMBRYOTOXON, INCLUDED
Gene map locus 20p12
8: *603693 Links
ZINC FINGER PROTEIN, MULTITYPE 2; ZFPM2
FOG2/AML1 FUSION GENE, INCLUDED
Gene map locus 8q23
9: #192430 GeneTests, Links
VELOCARDIOFACIAL SYNDROME
Gene map locus 22q11.2
10: #179613 Links
RECOMBINANT CHROMOSOME 8 SYNDROME
11: #188400 GeneTests, Links
DIGEORGE SYNDROME; DGS
DIGEORGE SYNDROME CHROMOSOME REGION, INCLUDED; DGCR, INCLUDED
Gene map locus 22q11.2
12: #214800 GeneTests, Links
CHARGE SYNDROME
Gene map locus 8q12.1, 7q21.1
13: 136760 GeneTests, Links
FRONTONASAL DYSPLASIA
14: 602249 Links
PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES
15: 601348 Links
ECTRODACTYLY OF LOWER LIMBS, CONGENITAL HEART DEFECT, AND MICROGNATHIA
16: 601322 Links
PORENCEPHALY, CEREBELLAR HYPOPLASIA, AND INTERNAL MALFORMATIONS
17: 600123 Links
ATRIOVENTRICULAR SEPTAL DEFECT WITH BLEPHAROPHIMOSIS AND ANAL AND RADIAL DEFECTS
18: 600001 Links
PANCREATIC HYPOPLASIA, CONGENITAL, WITH DIABETES MELLITUS AND CONGENITAL HEART DISEASE
19: 280000 Links
ZUNICH NEUROECTODERMAL SYNDROME
20: %274000 GeneTests, Links
THROMBOCYTOPENIA--ABSENT RADIUS SYNDROME
TETRAPHOCOMELIA-THROMBOCYTOPENIA SYNDROME, INCLUDED
Items 1 - 20 of 61
 
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